RGD:597696221 Rat Genome Database

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Variant: RGD:597696221 -  Homo sapiens

RGD ID: 597696221
ClinVar ID: CV3680293
Genic Status: GENIC
Type: SNV (SO:0001483) 
Associated Genes: IPCEF1  OPRM1  
Reference Nucleotide: T
Variant Nucleotide: C
Position
Assembly Chr Position
GRCh37 6 154,535,378
GRCh38 6 154,214,244
JBrowse: View Region in Genome Browser (JBrowse)
Model



HGVS Name(s)
Last Evaluated
Molecular Consequence
Clinical Significance
Trait Synonyms
LRG_1007t1:c.1165-32449T>C
NM_001008503.3:c.1165-32449T>C
NM_001394802.1:c.422A>G
NM_015553.3:c.422A>G
More... 		09/02/2024 intron variant uncertain significance AllHighlyPenetrant

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Database
Acc Id
Source(s)
ClinVar RCV004931922 CLINVAR
MedGen CN169374 CLINVAR
NCBI Gene IPCEF1 CLINVAR
  OPRM1 CLINVAR
OMIM 600018 CLINVAR
  619948 CLINVAR